Alerta De Seguridad para Sarns Malleable Dual-stage Venous Return Cannulae and Sarns Dual-stage Venous Return Cannulae

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Terumo Cardiovascular Systems Corporation.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2014-03-07
  • Fecha de publicación del evento
    2014-03-07
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: terumo sarns malleable dual-stage venous return cannulae and sarns dual-stage venous return cannulae medical device manufacturer, terumo cardiovascular systems corporation, has issued a medical device safety alert concerning all lots of sarns malleable dual-stage venous return cannulae and sarns dual-stage venous return cannulae with catalogue numbers 4934, 4934x, 4935, 4936, 4936x, 16472 and 16473. during in-process inspection, terumo cardiovascular systems (terumo cvs) identified exposed basket wire on certain product lots of sarns malleable dual-stage venous return cannulae and sarns dual-stage venous return cannulae. according to the manufacturer, the presence of exposed basket wire on the outside surface of the cannulae may be detected by the surgical team prior to patient exposure. if not detected, the exposed wire could result in tissue damage and a remote chance of air being introduced into the cardiopulmonary bypass circuit. the presence of exposed basket wire on the inside surface of the cannulae is more difficult to detect. the exposed wire could result in turbulence in blood flow increasing risk of hemolysis. terumo cvs has not received any reports of exposed basket wire from customers and there are no reported injuries from the observed defect. terumo cvs is recalling all affected cannulae. according to the local supplier, the affected products were not distributed to hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 07 march 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Terumo Sarns Malleable Dual-stage Venous Return Cannulae and Sarns Dual-stage Venous Return Cannulae
  • Manufacturer

Manufacturer